| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000226279 |
| Start |
15848556:15848556(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.857A>T |
| AA Mutation |
p.Gln286Leu(p.Q286L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000226279 |
| Start |
15838137:15838137(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.631T>C |
| AA Mutation |
p.Ser211Pro(p.S211P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000226279 |
| Start |
15840029:15840029(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.663T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |